Department of Immunology, Faculty of Medicine, Kindai University, Osaka, Japan.
Front Immunol. 2018 May 31;9:1214. doi: 10.3389/fimmu.2018.01214. eCollection 2018.
Tissue-resident memory T cells (T cells) are a population of immune cells that reside in the lymphoid and non-lymphoid organs without recirculation through the blood. These important cells occupy and utilize unique anatomical and physiological niches that are distinct from those for other memory T cell populations, such as central memory T cells in the secondary lymphoid organs and effector memory T cells that circulate through the tissues. CD8 T cells typically localize in the epithelial layers of barrier tissues where they are optimally positioned to act as sentinels to trigger antigen-specific protection against reinfection. CD4 T cells typically localize below the epithelial layers, such as below the basement membrane, and cluster in lymphoid structures designed to optimize interactions with antigen-presenting cells upon reinfection. A key feature of T populations is their ability to be maintained in barrier tissues for prolonged periods of time. For example, skin CD8 T cells displace epidermal niches originally occupied by γδ T cells, thereby enabling their stable persistence for years. It is also clear that the long-term maintenance of T cells in different microenvironments is dependent on multiple tissue-specific survival cues, although the specific details are poorly understood. However, not all T persist over the long term. Recently, we identified a new spatial niche for the maintenance of CD8 T cells in the lung, which is created at the site of tissue regeneration after injury [termed repair-associated memory depots (RAMD)]. The short-lived nature of RAMD potentially explains the short lifespans of CD8 T cells in this particular tissue. Clearly, a better understanding of the niche-dependent maintenance of T cells will be important for the development of vaccines designed to promote barrier immunity. In this review, we discuss recent advances in our understanding of the properties and nature of tissue-specific niches that maintain T cells in different tissues.
组织驻留记忆 T 细胞(T 细胞)是一群免疫细胞,它们存在于淋巴和非淋巴器官中,不会通过血液再循环。这些重要的细胞占据并利用独特的解剖和生理小生境,与其他记忆 T 细胞群体(如次级淋巴器官中的中央记忆 T 细胞和循环通过组织的效应记忆 T 细胞)不同。CD8 T 细胞通常定位于屏障组织的上皮层,在那里它们处于最佳位置,可以作为哨兵,触发针对再感染的抗原特异性保护。CD4 T 细胞通常位于上皮层下方,如基底膜下方,并聚集在设计用于优化与抗原呈递细胞相互作用的淋巴结构中。T 细胞群体的一个关键特征是它们能够在屏障组织中长时间维持。例如,皮肤 CD8 T 细胞取代了最初由 γδ T 细胞占据的表皮小生境,从而使其能够稳定地持续存在多年。显然,不同微环境中 T 细胞的长期维持依赖于多种组织特异性生存信号,尽管具体细节尚不清楚。然而,并非所有 T 细胞都能长期存在。最近,我们在肺中发现了一个新的 CD8 T 细胞维持的空间小生境,这个小生境是在组织损伤后的组织再生部位形成的(称为与修复相关的记忆库(RAMD))。RAMD 的短暂性质可能解释了该特定组织中 CD8 T 细胞的短暂寿命。显然,更好地理解依赖小生境的 T 细胞维持对于开发旨在促进屏障免疫的疫苗将是重要的。在这篇综述中,我们讨论了我们对维持不同组织中 T 细胞的组织特异性小生境的特性和性质的最新理解的进展。